The FDA perspectives on cleaning validation and areas of concern during regulatory inspections
The importance and underlying principles of cleaning validation and the requirements to have adequate cleaning procedures for manufacturing equipment in contact with the product
Prepare and defend your own cleaning validation approach/program and avoid costly delays and/or rejections by regulatory agencies
Cleaning validation procedures, protocols and reports that meet current FDA, WHO, PIC/S and EU regulations
Who should Attend
Quality professionals
Senior quality managers
Validation engineers
Production supervisors
Quality engineers
Process owners
Quality auditors
Past Events
The Life Cycle Approach to Cleaning Validation 2018 - 06-07 Dec 2018, Tampa, Florida, United States (80298)
Important
Please, check "The Life Cycle Approach to Cleaning Validation" official website for possible changes, before making any traveling arrangements
Event Categories
Business: Customer Service, Human Resources (HR), Management, Operations, Quality assurance
